首页> 外文期刊>西安医科大学学报(英文版) >ALTERATION IN CONTRACTILE RESPONSE TO NORADRENALINE,5-HYDROXYTRYPTAMINE,SARAFOTOXIN 6c,AND ANGIOTENSINⅡIN RAT MESENTERIC ARTERY DURING ORGAN CULTURE
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ALTERATION IN CONTRACTILE RESPONSE TO NORADRENALINE,5-HYDROXYTRYPTAMINE,SARAFOTOXIN 6c,AND ANGIOTENSINⅡIN RAT MESENTERIC ARTERY DURING ORGAN CULTURE

机译:器官培养对大鼠中动脉中肾上腺素,5-羟色胺,SARAFOTOXIN 6c和血管紧张素Ⅱ的收缩反应

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Objective To compare the vasoconstrictive effects of 9 mediators on fresh and incubated mesenteric arteries of rats. Methods The superior mesenteric artery of rat was removed and the endothelium was denuded. The vessels were cut into 1 mm long cylindrical segments and subjected to organ culture for 24 hours. Fresh or incubated segments were immersed into tissue baths and the concentration-response curves were obtained by cumulative administration of the vasoconstrictors. Results In fresh mesenteric artery, endothelin-1 (ET-1), 5-hydroxytryptamine (5-HT), noradrenaline (NA), 5-carboxamidotryptamine (5-CT), and angiotensinⅡ (AngⅡ) induced potent and sustained constrictions in a concentration-dependent manner. The contraction induced by sarafotoxin 6c (S6c) was weak, while bradykinin (BK), des-Arg-bradykinin (DA-BK), and human urotensinⅡ (hUT-II) showed no detectable contraction. The concentraion-response curves in order of slopes was ET-1, NA, 5-HT, 5-CT, and AngⅡ. The order of the maximum contractions was ET-1>NA=5-HT=5-CT>AngⅡ>S6c. After organ culture, the concentration-response curves induced by S6c, NA, and 5-HT were significantly increased, while that induced by AngⅡ was decreased as comparing to fresh arteries. BK contracted the artery only weakly. Conclusion Organ culture changed the phenotypes towards an increased efficacy of NA, 5-HT, S6c, and a reduced efficacy of AngⅡ, which is in accordance with the results of pharmacological characterization in some human vascular disease.
机译:目的比较9种介质对大鼠新鲜和温育肠系膜动脉的血管收缩作用。方法切除大鼠肠系膜上动脉,剥除内皮细胞。将容器切成1mm长的圆柱形部分,并进行器官培养24小时。将新鲜的或温育的段浸入组织浴中,并通过累积施用血管收缩剂获得浓度-反应曲线。结果在新鲜的肠系膜动脉中,内皮素-1(ET-1),5-羟基色胺(5-HT),去甲肾上腺素(NA),5-羧酰胺基色胺(5-CT)和血管紧张素Ⅱ(AngⅡ)诱导了大鼠的持续性强效收缩浓度依赖性的方式。 sarafotoxin 6c(S6c)诱导的收缩较弱,而缓激肽(BK),des-Arg-缓激肽(DA-BK)和人尿素II(hUT-II)则未显示可检测的收缩。浓度响应曲线的斜率依次为ET-1,NA,5-HT,5-CT和AngⅡ。最大收缩顺序为ET-1> NA = 5-HT = 5-CT>AngⅡ> S6c。器官培养后,与新鲜动脉相比,S6c,NA和5-HT诱导的浓度-反应曲线显着增加,而AngⅡ诱导的浓度-反应曲线降低。 BK仅微弱地收缩了动脉。结论器官培养改变了表型,使NA,5-HT,S6c的效力增加,而AngⅡ的效力下降,这与某些人类血管疾病的药理学表征结果相符。

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